钴
材料科学
阴极
功率密度
化学工程
小袋
跟踪(心理语言学)
离子
功率(物理)
化学
冶金
热力学
物理化学
地质学
有机化学
古生物学
物理
语言学
哲学
工程类
作者
Haifeng Yu,Zhihua Ren,Zhihong Wang,Hui Sun,Ling Chen,Hao Jiang,Chunzhong Li
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-10-16
卷期号:19 (42): 37314-37323
标识
DOI:10.1021/acsnano.5c12594
摘要
Layered Ni-rich Co-free cathodes offer compelling advantages in energy density and cost-effectiveness, but their practical deployment is significantly hindered by structural instability and sluggish charge transfer kinetics. Herein, we report a spinel Li1-xCoO2 surface-engineered LiNi0.92Mn0.05Al0.03O2 (Co-NMA) cathode with only ∼2000 ppm Co, in which the efficient utilization of trace Co dramatically enhances both structural integrity and interfacial reaction kinetics. Comprehensive in/ex situ spectrochemical analyses reveal that surface engineering effectively suppresses parasitic interface reactions with negligible O2/CO2 emission in the first charge process. Concurrently, spinel Li1-xCoO2 facilitates faster Li+ diffusion and electron transfer, resulting in lower electrochemical polarization and higher phase-transition reversibility. Consequently, the Co-NMA delivers a high reversible capacity of 225.3 mAh g-1 at 0.1C and an initial Coulombic efficiency of 93.4%. It retains 62.1% of its capacity retention even at 10C, greatly outperforming the corresponding quaternary NMCA (54.2%) and NMA (49.1%). In pouch-type full cells, the Co-NMA sustains an extended cycle life over 650 cycles with 80% capacity retention, far surpassing NMCA (<320 cycles) and the reported NMA-based cathodes.
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